药理学中重要名词解释Explanation of important nouns in pharmacologyWord格式.docx
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药理学中重要名词解释Explanation of important nouns in pharmacologyWord格式.docx
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Distribution:
theprocessbywhichdrugsareabsorbedandtransportedtotissuesthroughoutthecirculation.
Agingcurve:
acurveshowingtheeffectofadrugovertime.
Plasmahalf-life:
bloodconcentrationdecreasedbyhalfofthetime(t1/2).
Bioavailability:
-referstotherelativevolumeandvelocityabsorbedintothebodycirculationafterremovaloftheliver'
sfirstpass.F=A/D,Drepresentsthedosage,andAindicatesthedosetoenterthesystemiccirculation.
Absoluteoralbioavailability:
theratioofextravascularadministrationofAUCtoAUCafterintravenousinjection.
Therelativebioavailabilityofdrugdosageforms,theabsorptionrateofF=reagent,AUC/standardAUCcanbeusedasmedicine,drugqualityindexappraisal.
Zeroordereliminationkinetics:
whenthedruginthebodytoomuch,thebodywithitsmaximumabilitytoeliminatedrugs,eliminationratehasnothingtodowiththeC0,itwasataconstantspeed(alsoknownasquantitativeeasing);
plasmahalf-lifeisnotfixed,whenthebloodconcentrationdecreasedtobelowthemaximumeliminationcapacity,accordingtoafirst-orderelimination.
Firstorderkineticswithaconstantdrugeliminationratio,perunittimetoeliminatethedosedecreasewithtime,drughalf-lifehasnothingtodowiththelevelofconcentrationisconstant,adrugafterdrug,after5t1/2invivohasbeenbasicallyeliminated,every1t1/2administeredonce,afterupto5t1/2steadystate.
Steadystatebloodconcentration:
onceevery1t1/2,thedoseisequal,thenafter5t1/2,theamountofdrugsremovedandtheamountofdrugsenteringthebodyisequalto,thatis,steadystate.
Plasmaclearance:
drugperunittimesomevolumeoftheplasmaistoremovethebody,unitL/h,drugsforliverandkidneyeliminationrateofCL=RE(totaleliminationrate(/Cp)plasmadrugconcentrationatthetime).
Apparentvolumeofdistribution(Vd):
intravenousinjectionofacertainamountofdrugs,tobedistributedafterequilibrium,accordingtothemeasuredplasmaconcentration,calculatedtheamountofplasmathatthedrugshouldpossess.
Drugaction:
theinitialreactionbetweendrugsandthecellsofthebody.Itistheagent,themolecularreactionmechanism,andhasitsspecificity.
Pharmacologicaleffects:
theresultofdrugaction,theperformanceofthebody'
sresponse.
Adversereactions:
notconsistentwiththepurposeofmedication,andbringdiscomfortandpaintothepatient.
Drug-induceddisease:
adrug-induced,serious,ordifficulttorecoveradversereaction.
Sideeffects:
othereffectsoccurringattherapeuticdosesthatdonotcorrespondtothepurposeofthedrug.
Residualeffect:
theresidualpharmacologicaleffectafterthewithdrawalofserumconcentrationhasdroppedbelowthethresholdconcentration.
Withdrawalreaction:
suddenonsetofdiseaseresultingfromsuddendiscontinuationofthedrug(alsoknownasareboundreaction).
Toxicreaction:
ahazardousreactionthatoccurswhenthedosageistoolargeortoomuch.
Doseeffectrelationship:
theratioofpharmacologicaleffectstodosesatacertainconcentration.
Thedose-responsecurveineffectasordinateandconcentrationasabscissamapping,rectangularhyperbola.Thedrugconcentrationcanbeplottedbynumericalvalue,anditisatypicalsymmetricalScurve,whichisadoseeffectcurve.
Minimumeffectivedose:
thresholddoseforstiffnessinducedeffects.
Medianeffectivedose(ED50):
adoseofpositive(Qualitative)or50%maximaleffect(doseresponse)couldbeinducedin50%oftheanimals.
Medianmaximumeffectconcentration(EC50):
concentrationof50%maximumeffect.
Medianlethaldose(LD50):
adosethatcouldcausedeathin50%experimentalanimals.
Mediandoseofintoxication(TD50):
adosethatcouldcausepoisoningin50%laboratoryanimals.
Effectiveness:
continuetoincreasetheconcentrationordose,andtheeffectnolongercontinuestorise,referredtoaspotency(i.e.,maximumeffect).
Valencestrength:
therelativeconcentrationordosethatcancauseanequivalentreaction(usuallyusinga50%effectdose).
Structure-activityrelationship:
therelationshipbetweenthechemicalstructureofthedrugandthedrugeffect,whereinthechemicalstructureofthedrugconsistsofthebasicskeletonofthedrug,theactivegroup,thelengthofthesidechain,andthethree-dimensionalconfiguration.
Isakindofproteinfunction:
receptormediatedsignaltransduction,cantracesomechemicalidentificationofthesurroundingenvironment,thedrugbindsthroughtheintermediaryofsignaltransductionandamplification,cantriggerphysiologicalresponsesandpharmacologicaleffect.
Ligand:
asubstancethatcanspecificallybindtoreceptors.
Agonists:
ligandsthatactivatereceptorsarecalledagonists,andreceptoragonistshaveastrongaffinityforthecorrespondingreceptorsandhavestrongintrinsicactivity.
Anendogenoussubstance,suchasaneurotransmitter,hormone,oranactivesubstance,thatcanbindspecificallytothereceptor.
Antagonist:
aligandthatblocksreceptors,calledantagonists.
Competitiveantagonist:
adrugthatcompeteswithagonistsandreversiblycombineswiththereceptor.
Antagonistparameter(pA2):
thenegativelogarithmofthecompetitiveantagonistconcentrationrequiredtodoubletheagonistdoseandmaintaintheeffectunchanged.
Noncompetitiveantagonists:
drugsthatbindstronglytothereceptorandslowdownorirreversiblybindafterbinding;
inthedoseeffectcurve,EmaxdecreasesandKDdoesnotchange.
Partialagonist:
drugandreceptoraffinity,butintrinsicactivityislimited,withagonistandantagonistduality,whenagonistsinsmalldoses,theagonisteffectandsynergy,reachedEmax,andthereceptoragonistcompetitionisacompetitiveantagonismrelationship.
Drugequivalentandbiologicalequivalent:
theformerreferstotheamountofdrugscontainedindifferentpreparationsequal;
thelatterreferstothedifferentdosageofdrugscanachievethesameplasmaconcentrationoftheratioofthedose.
Synergy:
thecombinationoftwoormorethantwodrugsinordertoincreasetheeffectivenessofthetreatment.
Antagonism:
theuseofdrugsincombinationtoreduceadversedrugreactions.
Incompatibility:
referstothedruginvitrocompatibility,directphysiologicalinteractionandinfluencetheefficacy.
Rapidtolerance:
whenadrugisrepeatedseveraltimesoverashortperiodoftime,theefficacydiminishesuntilitdisappears.
Tolerance:
whencontinuousmedicationisused,thebody'
sresponsetothedrugisdecreased,andthedosageisincreasedtomaintaintheefficacy.
Drugresistance:
adecreaseinsusceptibilitytorepeatedchemotherapeuticagents,orresistance,topathogensortumorcells.
Habituation:
thefeelingofsubjectivediscomfortcausedbywithdrawal,andthecravingforcontinueduseofthedrug.
Addiction:
theuseofcertaindrugs,suchasmorphine,toinduceeuphoriaandseverewithdrawalsymptomsafterwithdrawal.
Dependence:
bothhabituationandaddiction,bothofwhicharesubjectiveandrequireacontinuoususeofdrugs,collectivelyreferredtoasdependence.
Drugabuse:
referstotheabsenceofdiseasebased,long-term,largenumberofselfmedication.
Individualdifferences:
thesamedrugmaynotachievethesamebloodconcentrationindifferentpatients,andthesamebloodconcentrationmaynotachievethesameeffect.Theindividualdrugresponseiscalledindividualdifference.
Ingestionof-1:
reuptakeofnorepinephrinebynerveterminals.
Ingestionof-2:
reuptakeofnorepinephrinebynonneuronaltissues,suchasmyocardiumandbloodvessels.
Spasmofaccommodation:
thepilocarpineeffectofciliarymuscleMreceptor,ciliarymusclecontraction,ligamentrelaxation,convexlens,myopiadiopterincreases,hyperopiablurredobjectclearly.
Controlparalysis:
AtropineciliarymusclebreakingMreceptor,ciliarymusclerelaxation,suspensoryligamenttension,flatlens,diopterdecreasedhyperopiamyopiablurredobjectclearly.
Depolarizingmusclerelaxants:
drugsthatcombinewiththeN2receptorproduceamorepersistentdepolarizationsimilartoAch,whichmakestheN2receptordonotrespondtoAchandrelaxskeletalmuscles.
Nondepolarizingmusclerelaxant:
acombinationofdrugsandN2receptorsthatcompetitivelyblockAchbyblockingN2receptorsandrelaxingskeletalmuscle.
Reversalofadrenergicaction:
alphablockerscanturnthepressoreffectofepinephrineintoahypotensiveeffect.
Intrinsicpseudosympatheticactivity:
somebetablockersbindtothebetareceptor,blockingthereceptorinvitroandpartlyactivatingthebetareceptor.
Thrombolyticdrugs:
fibrinolyticagents,activatedplasminfibrinolyticandthrombolysisforthetreatmentofacutethromboembolicdisease.
G-C
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